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Nutrition Impact on PRGF Treatment for Tendinopathy

Recruitingn/aAges 18 Years - 70 YearsAllI.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
NCT06536582 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Given the close correlation reported in the literature between onset and progression of tendon pathology in subjects affected by the alteration of metabolic disorders such as obesity, diabetes mellitus and lipidic metabolic alterations, with the present study the association between the nutritional state, metabolic profile and clinical outcome of patients following treatment with blood-derived orthobiological for shoulder tendinopathies will be evaluated. The primary aim of this study is to identify the proportion of tendinopatic patients responsive and non-responsive to treatment with "Platelet rich growth factors" PRGF at six months follow up and the correlation with their nutritional status.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Male and female * Age ≥18 years and ≤ 70 years * Patients presenting shoulder tendinopathy * Signing of the Informed Consent of the Regain observational study * Signature of informed consent of the present study. Exclusion Criteria: * Pregnancy (ascertained by self-declaration), breastfeeding * Inability to follow the study protocol * Heart, kidney, oncological disease * Neuropsychiatric disease * Other conditions that, at the discretion of the investigator or physician, exclude enrollement
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What it tests

  • Platelet rich growth factor injection (autologous product)
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Where

1 site
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Milan, Italy
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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